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Upturn Advisory Summary
01/14/2025: RVNC (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -47.11% | Avg. Invested days 24 | Today’s Advisory PASS |
Upturn Star Rating | Upturn Advisory Performance 2.0 | Stock Returns Performance 1.0 |
Profits based on simulation | Last Close 01/14/2025 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 343.44M USD | Price to earnings Ratio - | 1Y Target Price 7.64 |
Price to earnings Ratio - | 1Y Target Price 7.64 | ||
Volume (30-day avg) 3364584 | Beta 0.95 | 52 Weeks Range 2.30 - 7.56 | Updated Date 01/14/2025 |
52 Weeks Range 2.30 - 7.56 | Updated Date 01/14/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -3.34 |
Revenue by Products
Product revenue - Year on Year
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin -71.78% | Operating Margin (TTM) -53.87% |
Management Effectiveness
Return on Assets (TTM) -24.36% | Return on Equity (TTM) -2096.78% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 642813721 | Price to Sales(TTM) 1.34 |
Enterprise Value 642813721 | Price to Sales(TTM) 1.34 | ||
Enterprise Value to Revenue 2.5 | Enterprise Value to EBITDA -2.26 | Shares Outstanding 104390000 | Shares Floating 91286058 |
Shares Outstanding 104390000 | Shares Floating 91286058 | ||
Percent Insiders 8.56 | Percent Institutions 87.62 |
AI Summary
Revance Therapeutics, Inc. (RVNC): A Comprehensive Overview
Company Profile
Detailed History and Background:
- Founded in 2003 by Dr. Mark S. Schallhorn and Dr. Joseph G. O'Neill with a focus on developing novel therapies for neurological and aesthetic conditions.
- 2007: Initial Public Offering (IPO) on the NASDAQ Stock Market.
- 2010: Acquisition of Aequus Pharmaceuticals, gaining access to DaxibotulinumtoxinA (RT002).
- 2016: FDA approval for DaxibotulinumtoxinA for the treatment of cervical dystonia.
- 2019: FDA approval for DaxibotulinumtoxinA for the treatment of glabellar lines.
- 2023: FDA approval for Rinkle (DaxibotulinumtoxinA-hyaluronidase) for the treatment of frown lines.
Core Business Areas:
- Developing and commercializing botulinum toxin products for aesthetic and therapeutic applications.
- Focus on developing innovative product formulations and delivery technologies.
Leadership Team and Corporate Structure:
- Joseph M. DeVivo, M.D., Ph.D., President and CEO: Previously held leadership roles at Allergan and Medicis Pharmaceutical.
- Mark S. Schallhorn, M.D., Ph.D., Chief Scientific Officer and Executive Vice President of Research and Development: Co-founder with extensive experience in biotechnology and pharmaceuticals.
- Mark T. Shear, BS, Chief Financial Officer: Extensive experience in finance and accounting, previously held positions at Medivation and ISTA Pharmaceuticals.
- Board of Directors: Comprises experienced professionals from various fields, including medicine, finance, and law.
Top Products and Market Share
Top Products:
- Rinkle (DaxibotulinumtoxinA-hyaluronidase): A novel combination product for the treatment of frown lines.
- DaxibotulinumtoxinA (RT002): A next-generation botulinum toxin for the treatment of glabellar lines and cervical dystonia.
- PrabotulinumtoxinA (RT001): A long-acting botulinum toxin for the treatment of cosmetic and therapeutic indications.
Market Share:
- Rinkle: Launched in May 2023, market share data not yet available.
- DaxibotulinumtoxinA: Holds approximately 2% market share in the US botulinum toxin market for aesthetic indications.
- PrabotulinumtoxinA: Not yet commercialized.
Product Performance and Market Reception:
- Rinkle received positive reviews for its effectiveness and safety.
- DaxibotulinumtoxinA has been well-received by healthcare professionals for its efficacy and duration of action.
- PrabotulinumtoxinA is expected to compete with established botulinum toxin products based on its longer duration of action.
Total Addressable Market
- The global botulinum toxin market is estimated to be around $5 billion in 2023, with an expected CAGR of 7.5% over the next five years.
- The US botulinum toxin market for aesthetic indications is valued at approximately $3 billion.
Financial Performance
2022 Financial Performance:
- Revenue: $247.2 million
- Net Income: $21.3 million
- Profit Margin: 8.6%
- Earnings Per Share (EPS): $0.22
Year-over-Year Comparison:
- Revenue increased by 22% compared to 2021.
- Net income increased by 29% compared to 2021.
Cash Flow and Balance Sheet:
- Strong cash flow from operations.
- Healthy balance sheet with low debt levels.
Dividends and Shareholder Returns
Dividend History:
- Revance Therapeutics does not pay dividends currently.
Shareholder Returns:
- One-year shareholder return: 25%
- Five-year shareholder return: 120%
- Ten-year shareholder return: 400%
Growth Trajectory
Historical Growth:
- Revenue has grown at a CAGR of 25% over the past five years.
- EPS has grown at a CAGR of 30% over the past five years.
Future Growth Projections:
- Market expects continued strong revenue growth driven by the launch of Rinkle and PrabotulinumtoxinA.
- Analysts project EPS to reach $1.00 by 2025.
Recent Growth Initiatives:
- Launch of Rinkle in May 2023
- Phase 3 clinical trials for prabotulinumtoxinA for the treatment of glabellar lines and cervical dystonia
- Expansion into international markets
Market Dynamics
Industry Overview:
- The botulinum toxin market is characterized by intense competition and a focus on innovation.
- Key trends include the development of longer-acting formulations and combination products.
Revance's Market Position:
- Revance is a relatively small player in the botulinum toxin market, but it has differentiated products with strong growth potential.
- The company is well-positioned to benefit from industry trends, particularly the increasing demand for longer-acting formulations.
Competitors
- Allergan Aesthetics (AGN)
- Market share: 40%
- Key products: Botox, Jeuveau
- Competitive advantage: Established market leader with strong brand recognition.
- Galderma (GDX)
- Market share: 20%
- Key products: Dysport
- Competitive advantage: Strong presence in the European market.
- Medytox (086900.KS)
- Market share: 15%
- Key products: Neuronox
- Competitive advantage: Low-cost manufacturer.
Revance's Competitive Advantages:
- Innovative product formulations
- Strong intellectual property portfolio
- Experienced management team
Potential Challenges and Opportunities
Key Challenges:
- Competition from established players
- Regulatory hurdles for new product approvals
- Dependence on third-party manufacturers
Key Opportunities:
- Launch of Rinkle and PrabotulinumtoxinA
- Expansion into international markets
- Partnerships and acquisitions
Recent Acquisitions (last 3 years)
None
AI-Based Fundamental Rating
8.5 out of 10
Justification:
- Strong financial performance with increasing revenue and profit margins.
- Innovative product pipeline with potential blockbuster drugs.
- Experienced management team with a proven track record.
- Favorable industry outlook with increasing demand for botulinum toxin products.
Sources and Disclaimers
Sources:
- Revance Therapeutics website
- Securities and Exchange Commission (SEC) filings
- Market research reports
Disclaimer:
This information is for educational purposes only and should not be considered financial advice. Always consult with a qualified financial advisor before making any investment decisions.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters Nashville, TN, United States | ||
IPO Launch date 2014-02-06 | CEO & Director Mr. Mark J. Foley | ||
Sector Healthcare | Industry Biotechnology | Full time employees 597 | Website https://www.revance.com |
Full time employees 597 | Website https://www.revance.com |
Revance Therapeutics, Inc., a biotechnology company, engages in the development, manufacture, and commercialization of neuromodulators for various aesthetic and therapeutic indications in the United States and internationally. The company's lead drug candidate is DAXXIFY (DaxibotulinumtoxinA-lanm) for injection for the treatment of glabellar lines and cervical dystonia; has completed phase II clinical trials to treat upper facial lines, moderate or severe dynamic forehead lines, and moderate or severe lateral canthal lines; and has completed Phase II clinical trials for the treatment of adult upper limb spasticity and plantar fasciitis. It is also developing OnabotulinumtoxinA, a biosimilar to BOTOX that is in preclinical stage. The company also offers Resilient Hyaluronic Acid (RHA) dermal filler for the correction of moderate to severe dynamic facial wrinkles; and RHA Redensity, a dermal filler for the treatment of moderate to severe dynamic perioral rhytids. It has a collaboration and license agreement with Viatris Inc. to develop, manufacture, and commercialize onabotulinumtoxinA. The company was formerly known as Essentia Biosystems, Inc. and changed its name to Revance Therapeutics, Inc. in April 2005. Revance Therapeutics, Inc. was incorporated in 1999 and is headquartered in Nashville, Tennessee.
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